United States · FDA National Drug Code directory
Risperidone
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69238-2109_1da64781-e6c1-4e8d-a795-6ef0f9a43284
- Product NDC
- 69238-2109
- Form
- TABLET
- Composition / generic term
- Risperidone
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210801
- Source listing expiry
- 20271231
Source-listed ingredients
- RISPERIDONE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BLISTER PACK (69238-2109-5) · 69238-2109-5
- 60 TABLET in 1 BOTTLE (69238-2109-6) · 69238-2109-6
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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